Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605222 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KCNMB3 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||||||||
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Global
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Caucasian
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CEPH (CEU) - Not Available | |||||||||
EAS
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African American
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YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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KCNMB3 - potassium calcium-activated channel subfamily M regulatory beta subunit 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163677.1 | 643 | Missense Mutation | GAT,GGT | D,G 42 | NP_001157149.1 | |
NM_014407.3 | 643 | Missense Mutation | GAT,GGT | D,G 44 | NP_055222.3 | |
NM_171828.2 | 643 | Missense Mutation | GAT,GGT | D,G 42 | NP_741979.1 | |
NM_171829.2 | 643 | Missense Mutation | GAT,GGT | D,G 22 | NP_741980.1 | |
NM_171830.1 | 643 | Missense Mutation | GAT,GGT | D,G 40 | NP_741981.1 |
Set Membership: |
HapMap Validated |